• One Case of BRCA2 Germline Mutation Ovarian Cancer Mother and Carrier Daughter found by Genetic Coun...

• Lee Eun-Jung

• Jeong Hee-Jong, Kim Min-Kyu

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 124 ~ 127

• Height and Bone Phenotype of 22q11.2 Deletion Syndrome: Lessons from the Gene Analysis of Three Case...

• Kim Bu-Kyung

• Sohn Young-Bae, Park Sang-Jin, Yim Shin-Young, Chung Yoon-Sok

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 120 ~ 123

• A Rare Case of Double Trisomy Mosaicism: 47,XXX/47,XX,+8

• Lee Jae-Hee

• Kim Heung-Sik, Ha Jung-Sook

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 117 ~ 119

• A Neonatal Form of Alexander Disease Presented with Intractable Seizures and Obstructive Hydrocephal...

• Yoo Il-Han

• Hong Won-Gi, Lim Byung-Chan, Hwang Hee, Chae Jong-Hee, Kim Ki-Joong, Hwang Yong-Seung

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 113 ~ 116

• A Novel Insertion in Exon 23 of the TCOF1 Gene in a Newborn Infant with Treacher Collins Syndrome

• Yang Ji-Hyeon

• Cha Hyo-Hyun, Yoon Hye-Sun

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 109 ~ 112

• Paracentric Inversions Found in Prenatal Diagnosis

• Lee Shin-Yeong

• Lee Bom-Yi, Park Ju-Yeon, Choi Eun-Young, Lee Yeon-Woo, Oh Ah-Rum, Ryu Hyun-Mee, Park So-Y...

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 104 ~ 108

• Prenatal Diagnosis of Chromosome 22q11.2 Deletions: Experiences in a Single Institution

• Chae Yong-Hwa

• Kwak Dong-Wook, Kim Moon-Young, Park So-Yeon, Lee Bom-Yi, Lee Yeon-Woo, Lee Young-Ho, Song...

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 99 ~ 103

• Female Carriers of Duchenne Muscular Dystrophy

• Cho Yu-Na

• Choi Young-Chul

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 94 ~ 98

• Alexander Disease

• Kang Ji-Hae

• Hong Seung-Jee, Kim Doo-Kwun

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 88 ~ 93

• Pseudohypoaldosteronism Type 1

• Cheong Hae-Il

• ´ëÇÑÀÇÇÐÀ¯ÀüÇÐȸÁö   2013  Volume.10  No.2 81 ~ 87